Applications of mRNA Delivery in Cancer Immunotherapy.

IF 6.6 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY
International Journal of Nanomedicine Pub Date : 2025-03-17 eCollection Date: 2025-01-01 DOI:10.2147/IJN.S500520
Xiaoyu Pan, Yang-Wen-Qing Zhang, Caixia Dai, Junyu Zhang, Minghe Zhang, Xi Chen
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引用次数: 0

Abstract

Cancer treatment is continually advancing, with immunotherapy gaining prominence as a standard modality that has markedly improved the management of various malignancies. Despite these advancements, the efficacy of immunotherapy remains variable, with certain cancers exhibiting limited response and patient outcomes differing considerably. Thus, enhancing the effectiveness of immunotherapy is imperative. A promising avenue is mRNA delivery, employing carriers such as liposomes, peptide nanoparticles, inorganic nanoparticles, and exosomes to introduce mRNA cargos encoding tumor antigens, immune-stimulatory, or immune-modulatory molecules into the tumor immune microenvironment (TIME). This method aims to activate the immune system to target and eradicate tumor cells. In this review, we introduce the characteristics and limitations of these carriers and summarize the application and mechanisms of currently prevalent cargos in mRNA-based tumor treatment. Additionally, given the significant clinical application of immune checkpoint inhibitors (ICIs) and chimeric antigen receptor (CAR)-based cell therapies in solid tumors (including melanoma, non-small-cell lung cancer, head and neck squamous cell carcinoma, triple-negative breast cancer, gastric cancer) and leukemia, which have become first-line treatments, we highlight and discuss recent progress in combining mRNA delivery with ICIs, CAR-T, CAR-NK, and CAR-macrophage therapies. This combination enhances the targeting capabilities and efficacy of ICIs and CAR-cell-based therapies, while also mitigating the long-term off-target toxicities associated with conventional methods. Finally, we analyze the limitations of current mRNA delivery systems, such as nuclease-induced mRNA instability, immunogenicity risks, complex carrier production, and knowledge gaps concerning dosing and safety. Addressing these challenges is crucial for unlocking the potential of mRNA in cancer immunotherapy. Overall, exploring mRNA delivery enriches our comprehension of cancer immunotherapy and holds promise for developing personalized and effective treatment strategies, potentially enhancing the immune responses of cancer patients and extending their survival time.

mRNA传递在肿瘤免疫治疗中的应用。
癌症治疗正在不断进步,免疫治疗作为一种标准治疗方式,已显著改善了各种恶性肿瘤的治疗。尽管取得了这些进展,但免疫疗法的疗效仍然不稳定,某些癌症的反应有限,患者的预后差异很大。因此,提高免疫治疗的有效性势在必行。一个有前景的途径是mRNA递送,利用载体如脂质体、肽纳米颗粒、无机纳米颗粒和外泌体将编码肿瘤抗原、免疫刺激或免疫调节分子的mRNA载物引入肿瘤免疫微环境(TIME)。这种方法旨在激活免疫系统来靶向和根除肿瘤细胞。在本文中,我们介绍了这些载体的特点和局限性,并总结了目前流行的货物在mrna肿瘤治疗中的应用和机制。此外,鉴于免疫检查点抑制剂(ICIs)和基于嵌合抗原受体(CAR)的细胞疗法在实体肿瘤(包括黑色素瘤、非小细胞肺癌、头颈部鳞状细胞癌、三阴性乳腺癌、胃癌)和白血病中的重要临床应用,这些疗法已成为一线治疗方法,我们强调并讨论了mRNA递送与ICIs、CAR- t、CAR- nk和CAR-巨噬细胞疗法联合的最新进展。这种组合增强了ICIs和car细胞疗法的靶向能力和疗效,同时也减轻了与传统方法相关的长期脱靶毒性。最后,我们分析了当前mRNA传递系统的局限性,如核酸酶诱导的mRNA不稳定性、免疫原性风险、复杂载体的生产以及有关剂量和安全性的知识差距。解决这些挑战对于释放mRNA在癌症免疫治疗中的潜力至关重要。总的来说,探索mRNA的传递丰富了我们对癌症免疫治疗的理解,并有望开发个性化和有效的治疗策略,潜在地增强癌症患者的免疫反应并延长他们的生存时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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